Phe-Pro
Phe-Pro structure
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Common Name | Phe-Pro | ||
|---|---|---|---|---|
| CAS Number | 7669-65-0 | Molecular Weight | 262.30400 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C14H18N2O3 | Melting Point | 127-129℃ | |
| MSDS | Chinese USA | Flash Point | N/A | |
Use of Phe-Pro(S)-1-((S)-2-Amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid is a proline derivative[1]. |
This table lists Chinese names, IUPAC names and various aliases of this chemical substance.
| Name | 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid |
|---|---|
| Synonym | More Synonyms |
This table contains bioactivity, target information and biological‑assay experimental data of this compound.
| Description | (S)-1-((S)-2-Amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid is a proline derivative[1]. |
|---|---|
| Related Catalog | |
| In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
| References |
This table shows physicochemical parameters including melting point, boiling point, density, solubility and optical rotation. Missing data is marked as N/A.
| Melting Point | 127-129℃ |
|---|---|
| Molecular Formula | C14H18N2O3 |
| Molecular Weight | 262.30400 |
| Exact Mass | 262.13200 |
| PSA | 83.63000 |
| LogP | 1.27020 |
| InChIKey | WEQJQNWXCSUVMA-RYUDHWBXSA-N |
| SMILES | NC(Cc1ccccc1)C(=O)N1CCCC1C(=O)O |
| Storage condition | -20°C |
This table provides MSDS information including hazard classification, first‑aid, fire‑fighting, spill handling, operation and storage instructions.
This table covers safety warnings, protective measures, incompatible substances and disposal guidelines for this compound.
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xi |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3.0 |
| HS Code | 2933990090 |
This table presents publicly reported synthetic routes, reaction conditions, reactants and product information of the compound.
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Phe-Pro CAS#:7669-65-0 |
| Literature: Xiang, Dao Feng; Patskovsky, Yury; Xu, Chengfu; Fedorov, Alexander A.; Fedorov, Elena V.; Sisco, Abby A.; Sauder, J. Michael; Burley, Stephen K.; Almo, Steven C.; Raushel, Frank M. Biochemistry, 2010 , vol. 49, # 31 p. 6791 - 6803 |
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Phe-Pro CAS#:7669-65-0
Detail
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| Literature: Yan; Ho; Hou Bioscience, biotechnology, and biochemistry, 1992 , vol. 56, # 5 p. 704 - 707 |
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Phe-Pro CAS#:7669-65-0
Detail
Learn More
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| Literature: Heiduschka; Dittrich; Heins; Neubert; Barth Pharmazie, 1989 , vol. 44, # 11 p. 778 - 780 |
This table lists upstream starting materials and downstream derivative products related to this chemical.
| Precursor 2 | |
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| DownStream 0 | |
This table shows customs‑related data including HS‑code, tariff and regulatory conditions for import and export.
| HS Code | 2933990090 |
|---|---|
| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
This table lists relevant public references with title, journal and publication metadata for this compound.
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Determination of the cis-trans isomerization barrier of several L-peptidyl-L-proline dipeptides by dynamic capillary electrophoresis and computer simulation.
Electrophoresis 22 , 2409-2415, (2001) Dynamic capillary electrophoresis (DCE) and computer simulation of the elution profiles with the theoretical plate and the stochastic model has been applied to determine the isomerization barriers of ... |
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Biological evaluation of RBx-0128, a potent and selective dipeptidyl peptidase-IV inhibitor in type 2 diabetes genetic model.
Indian J. Pharmacol. 44(6) , 759-64, (2012) Dipeptidyl peptidase IV (DPP-IV) inhibition to modulate the incretin effect is a proven strategy to treat type 2 diabetes mellitus. The present study describes the pharmacological profile of a novel D... |
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Determination of the cis-trans isomerization barrier of enalaprilat by dynamic capillary electrophoresis and computer simulation.
Electrophoresis 25 , 318-323, (2004) Dynamic capillary electrophoresis (DCE) and computer simulation of the elution profiles with the stochastic model has been applied to determine the isomerization barriers of the angiotensin converting... |
This table contains target information, in‑vitro & in‑vivo assay data for this compound.
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Name: Inhibition of ACE (unknown origin)
Source: ChEMBL
Target: Angiotensin-converting enzyme
External Id: CHEMBL3363246
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Name: TP_TRANSPORTER: uptake in Xenopus laevis oocytes
Source: ChEMBL
Target: Solute carrier family 15 member 1
External Id: CHEMBL2077579
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Name: Inhibition constant (Ki) for human intestinal peptide carrier
Source: ChEMBL
Target: Solute carrier family 15 member 1
External Id: CHEMBL699705
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Name: Inhibition of rabbit lung ACE preincubated for 5 mins by spectrophotometric assay
Source: ChEMBL
Target: Angiotensin-converting enzyme
External Id: CHEMBL1810334
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This table collects all English aliases, systematic names and CAS‑related synonyms of the compound.
| L-phenylalanyl-L-proline |
| Phe-Pro |
| Phenylalanylproline |
| H-Phe-Pro-OH |
| L-Phe-L-Pro |
| L-phenylalanine-L-Proline |
This section contains frequently‑asked‑questions about this compound, including basic parameters, properties, storage conditions and corresponding answers.
| Q: What is the English name of 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid? |
| A: The English name of 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid is 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid. |
| Q: What is the CAS number of 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid? |
| A: CAS number of 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid is 7669-65-0. |
| Q: What are the uses of 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid? |
| A: Main uses of 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid: (S)-1-((S)-2-Amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid is a proline derivative[1]. |
| Q: What English synonyms does 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid have? |
| A: English synonyms of 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid: L-phenylalanyl-L-proline, Phe-Pro, Phenylalanylproline, H-Phe-Pro-OH, L-Phe-L-Pro, L-phenylalanine-L-Proline. |
| Q: What is the molecular weight of 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid? |
| A: Molecular weight of 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid is 262.30400. |
| Q: What is the molecular formula of 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid? |
| A: Molecular formula of 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid is C14H18N2O3. |
| Q: What is the LogP of 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid? |
| A: LogP of 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid is 1.27020. |
| Q: What are the storage conditions for 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid? |
| A: Storage conditions for 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid: -20°C. |
| Q: What is the InChIKey of 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid? |
| A: InChIKey of 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid is WEQJQNWXCSUVMA-RYUDHWBXSA-N. |
| Q: What are the upstream materials of 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid? |
| A: Related upstream materials(CAS) of 1-(2-amino-3-phenylpropanoyl)pyrrolidine-2-carboxylic acid: 72122-62-4;56-40-6. |
This table lists manufacturers and suppliers of this compound, including vendor names and product supply reference information.
| Shanghai Nianxing Industrial Co., Ltd |